Biomet, Inc.: Device Recall
Recall #Z-0212-2026 · 09/23/2025
Class II: Risk
Recall Details
- Recall Number
- Z-0212-2026
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- Biomet, Inc.
- Status
- Ongoing
- Date Initiated
- 09/23/2025
- Location
- Warsaw, IN, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 98 units
Reason for Recall
There is a potential for a missing slotted button assembly in one lot of ZipTight, Acute AC Joint Implant, Single Ziploop
Product Description
BIOMET ZipTight, Acute AC Joint Implant, Single Ziploop , Model/Catalog Number: 904834; Fixation System for AC Joint Repair
Distribution Pattern
Refer to the attached ZFA 2025-00166_Initial Consignee List and ZFA 2025-00166_Initial Distribution History containing the distribution and the identification of the domestic consignees.
Other Recalls by Biomet, Inc.
- Class II: Risk 09/09/2025
- Class II: Risk 10/21/2024
- Class II: Risk 05/17/2024
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.